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Charles River Launches Viral Vector Tech Transfer Program to Safeguard Gene Therapy Development
Fast Track and Modular frameworks facilitate product development continuity via seamless process transfer to the Company’s viral vector Center of Excellence
Charles River’s viral vector tech transfer program offers phase-appropriate and customizable frameworks to yield exceptional stability, helping to avoid costly and time-consuming program delays. The Fast Track framework enables a streamlined approach to tech transfer when no process changes are required. The Modular framework facilitates fully customizable tech transfer for more complex scenarios when processes are not yet fully developed or process changes are required, such as switching a cell line, plasmid supply, and/or assay/analytical development, bolstered by Charles River’s premier testing platform. Both frameworks enable reliable transfer to the viral vector CoE, avoiding preventable delays and safeguarding continued program success.
With full-scale, in-house plasmid DNA and viral vector production capabilities, Charles River can efficiently manage tech transfers for a wide range of viral vectors, such as adeno-associated virus (AAV), adenovirus, lentivirus, and retrovirus. Once technology transfer has been initiated, developers gain access to Charles River’s integrated concept to cure portfolio, spanning discovery through safety assessment and commercialization.
Explore Flexible Tech Transfer at the
Charles River will showcase its viral vector tech transfer framework at the
During the conference, Ramin Baghirzade, PhD, Senior Director, Global Head Commercial, Gene Therapy CDMO Services, will take to the
Viral Vector Manufacturing Services
Charles River’s viral vector center of excellence offers viral vector tech transfer and manufacturing to support any stage of the drug development lifecycle, from research-grade viral vector manufacturing for in vitro and in vivo studies to commercial-scale GMP manufacturing. In recent years, the Company has significantly broadened its cell and gene therapy portfolio with several acquisitions and expansions to simplify complex supply chains and meet the growing demand for plasmid DNA, viral vector, and cell therapy services.
Watch the latest expert roundtable, Streamlining Cell and Gene Therapy Scalability: Progress Towards a Gold Standard, on-demand, and gain insights from a development, manufacturing, and testing perspective: https://bit.ly/3UCX8LW
Approved Quotes
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“A reliable, end-to-end CDMO is critical for continuity of supply and program efficiency. Charles River’s viral vector technology transfer program provides gene therapy developers with a cohesive concept-to-cure solution portfolio, fine tuned over decades supporting advanced therapy clients from discovery to commercialization and every step in between.” –
Kerstin Dolph , Corporate Senior Vice President, Global Manufacturing, Charles River - “Viral vector manufacturing and tech transfer is complex, requiring precision and accuracy to avoid costly and time-consuming program delays. Meticulously built to provide a seamless tech transfer at any phase, the viral vector tech transfer program provides stability in times of change.” – Ramin Baghirzade, PhD, Senior Director, Global Head Commercial, Gene Therapy CDMO Services, Charles River
About Charles River
Charles River provides essential products and services to help pharmaceutical and biotechnology companies, government agencies and leading academic institutions around the globe accelerate their research and drug development efforts. Our dedicated employees are focused on providing clients with exactly what they need to improve and expedite the discovery, early-stage development and safe manufacture of new therapies for the patients who need them. To learn more about our unique portfolio and breadth of services, visit www.criver.com.
View source version on businesswire.com: https://www.businesswire.com/news/home/20240530700445/en/
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781.222.6455
todd.spencer@crl.com
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